Medical Oncologist, Victoria Island Cancer Center, Victoria, British Columbia, Canada, 2410 Lee Avenue V8R 6V5.
Clin Med Insights Oncol. 2011;5:365-79. doi: 10.4137/CMO.S4259. Epub 2011 Nov 9.
Just over a decade ago, gastrointestinal tumours were a poorly understood mesenchymal neoplasm unsuccessfully treated with chemotherapy. Cytotoxic therapy for advanced disease yielded response rates of 10% and median survival of just 18 months. However, the discovery of KIT and platelet derived growth factor receptor alpha (PDGFRA) mutations as oncogenic drivers of most gastrointestinal tumours, paved the way for targeted therapy. Imatinib mesylate, a tyrosine kinase inhibitor, produces a clinical benefit rate (complete response, partial response, and stable disease) of more than 80% in metastatic setting and a median survival of 57 months. Imatinib is now also approved in adult patients following resection of KIT-positive GIST. Major insights into the mechanism of action of imatinib, unique pharmacokinetics, drug resistance, and management of low grade but chronic adverse effects continue to be made.
就在十多年前,胃肠道肿瘤是一种了解甚少的间叶性肿瘤,用化疗治疗效果不佳。晚期疾病的细胞毒性治疗的反应率为 10%,中位生存期仅为 18 个月。然而,发现 KIT 和血小板衍生生长因子受体α(PDGFRA)突变是大多数胃肠道肿瘤的致癌驱动因素,为靶向治疗铺平了道路。甲磺酸伊马替尼是一种酪氨酸激酶抑制剂,在转移性环境中产生超过 80%的临床受益率(完全缓解、部分缓解和稳定疾病),中位生存期为 57 个月。甲磺酸伊马替尼现在也被批准用于 KIT 阳性 GIST 切除后的成年患者。对伊马替尼作用机制、独特药代动力学、耐药性以及对低级别但慢性不良反应的管理的主要认识仍在不断取得进展。